ライフサイエンスコーパス: classical

1 time reduced in the same ratio compared to a classical acquisition at the same resolution.

2 (MFG and ITG) and resistant (cerebellum) to classical AD pathology.

3 Revisiting classical aesthetics in the light of recent psychologica

4 ta Stone, the Hechtian Hypothesis translates classical AGP function as a Ca(2+) capacitor, pollen tub

5 Projections from the "classical" agranular, disgranular, and granular insular

6 al spin chain with the most memory-efficient classical algorithm known requires infinite memory, whil

7 g a simple LRU cache model, we show that the Classical algorithm of Nussinov has the highest number o

8 r the very different stabilities between the classical alkyne complexes of Pt(II) and their drastical

9 gion was comprehensively studied by imputing classical alleles and polymorphic amino acid positions.

10 s of the nitronyl group in comparison to the classical alpha-phenyl-N-tert-butylnitrone (PBN).

11 Complement C3 is important for the classical, alternative, and lectin pathways of complemen

12 proteins comprise three activation pathways (classical, alternative, and lectin) and a terminal cytol

13 tasks of entanglement transformation and its classical analog of secrecy manipulation.

14 ses and microwave excitations, we report the classical analogue of Rabi oscillations in ensemble-aver

15 d type of quantum stereodynamics that has no classical analogue or interpretation.

16 Here authors perform classical and accelerated molecular dynamics simulations

17 tains diverse cancer phenotypes via distinct classical and alternative signaling pathways, with impli

18 consumption by as much as 88.8% relative to Classical and by as much as 56.3% and 57.8% relative to

19 Exploratory classical and compositional data analyses showed that th

20 , and plasma metabolomics from subjects with classical and early-onset forms of type 2 diabetes (T2D)

21 Thus, the classical and evolutionarily conserved POMT O-mannosylat

22 erous palaeodictyopteran insect nymphs using classical and high-tech techniques.

23 et was generated using highly purified human classical and nonclassical monocyte subsets from a clini

24 Both classical and nonclassical monocytes, but not CD1c(+) DC

25 Highlighting conceptual differences with classical and quantum computation, we demonstrate how th

26 een studied in the condensed phase with both classical and quantum methods using explicitly and impli

27 We perform here large-scale classical and quantum molecular simulations to study the

28 into vortex beams have found applications in classical and quantum optics.

29 ideal for space communications, both in the classical and quantum regimes.

30 hanism for complement activation through the classical and the related lectin pathway.

31 t the transition between thermal activation (classical) and tunneling (quantum) regimes exhibits univ

32 S, whom we classified into 2 groups: type 1 (classical) and type 2 (secondary) iSS.

33 acteria causing it, their resistance against classical antibiotics, the formation of a biofilm and th

34 rived dendritic cells (moDCs) that represent classical antigen-presenting cells and we aimed at study

35 tom bit represents the ultimate limit of the classical approach to high-density magnetic storage medi

36 In contrast to classical approaches starting from thiols or their deriv

37 ious diseases that have proven refractory to classical approaches.

38 he motion of each atom in a protein based on classical approximations of interatomic forces, giving r

39 ein ATG5 and the kinase ULK1 are involved in classical autophagy, while LC3-associated phagocytosis i

40 e intraepithelial lymphocytes (IELs) lacking classical B-, T-, and natural killer (NK)-cell lineage m

41 grees or narrower, and transmission matching classical ballistic predictions.

42 It differs from classical Bayesian methods in which a classification mod

43 portantly, MAJIQ-SPEL is able to handle both classical (binary) and complex, non-binary, splicing var

44 known HCA subtypes through identification of classical biomarkers in each HCA subgroup.

45 m sensing regulator HapR, which is absent in classical biotype strains.

46 Restoring HapR expression in classical biotype V. cholerae repressed vieSAB transcrip

47 We show that in classical biotype V. cholerae, LeuO cooperates with the

48 ne in VieA specific activity compared to the classical biotype.

49 holerae El Tor that is not functional in the classical biotype.

50 The El Tor and classical biotypes of O1 V. cholerae show striking diffe

51 ompared 2 models of character evolution, the classical "Brownian motion" model and another model ("Or

52 Blocking either classical calpain or atypical small optic lobe (SOL) cal

53 Associative LTF is blocked by dn classical calpain, whereas non-associative LTF is blocke

54 eir properties based on macroscopic theories-classical capillarity for intrusion and classical nuclea

55 These systems connect with classical cardiovascular organs, such as the heart and v

56 Classical cardiovascular risk factors were self-reported

57 The S-H/pi interaction differs from classical cation/pi interactions by the preferential ali

58 cent findings suggest that components of the classical cell death machinery also have important non-c

59 ul for quantum gate operations, but also for classical charge and information transfer processes.

60 liger oxidations are difficult to achieve by classical chemical means, particularly when large, funct

61 Formyl peptide receptor 2 (FPR2), a classical chemoattractant receptor of G-protein-coupled

62 Classical complement activation was inhibited by pretrea

63 Upstream inhibition of classical complement may be therapeutic to dampen mononu

64 Specific inhibition of the classical complement pathway using TNT003 or C1q-deplete

65 lement factor 1q (C1q) and activation of the classical complement pathway.

66 achine, initiating an approach to reversible classical computation based on state-of-the-art implemen

67 Mappings of classical computation onto statistical mechanics models

68 Here we map universal reversible classical computations onto a planar vertex model that e

69 s how we can reliably compare the power of a classical computer to the power of a quantum computer.

70 ems here are not yet large enough to eclipse classical computers, this experiment exposes critical fa

71 machine learning that is faster than that of classical computers.

72 implementations will differ markedly from in classical computing.

73 n this process can be explained according to classical concepts of crystal nucleation and growth, and

74 r studies have both transformed and expanded classical concepts of receptor pharmacology and have beg

75 ody (MB) is critically involved in olfactory classical conditioning, and cAMP signaling molecules are

76 tudying the molecular and cellular basis for classical conditioning, based on its ability to associat

77 During classical conditioning, we observed opposite dynamics in

78 In some special cases, classical conservation laws are broken at the quantum le

79 cule collisions can often be understood from classical considerations, in which the particles are rep

80 plative dyads elicited engagement similar to classical contemplative practices and increased perceive

81 ctors, in a variant of the Ray-Dutt twist of classical coordination chemistry, which we call the pter

82 quantum discord like measurements as well as classical correlations between the qubits.

83 superiority of quantum annealers over their classical counterparts has been ongoing since the incept

84 hey generally require less memory than their classical counterparts.

85 Unlike classical covalent polymers, one-dimensionally (1D) elon

86 cortical macro-parcellation not predicted by classical cytoarchitectonic definitions of cortical area

87 llow seed and white flower phenotypes of the classical d mutation was found to be due to one nucleoti

88 this case, this work presents evidence that classical d-block redox chemistry can be performed rever

89 plasmacytoid DC (pDC) and antigen-presenting classical DC (cDC) is controlled by the E protein transc

90 analysis suggested that RelB is required for classical dendritic cell (cDC) development based on a se

91 n of the essential autophagy protein ATG5 in classical dendritic cells (DCs), which are present at lo

92 These cells' local circuits differ from classical descriptions of L4B circuits in both the lamin

93 Classical descriptions of the hypothalamus divide it int

94 In analogy with the classical destabilising influence of the ice-albedo feed

95 ruses protection against temperature and the classical disinfection treatments used in drinking water

96 and grasping synergies, suggesting that this classical division of reach and grasp in PMd and PMv, re

97 Classical drug-choice assessments, which offer drug-cons

98 act as hosts of diverse guests ranging from classical dyes to drugs and quantum dots, allowing chang

99 ed to be unimportant; (3) obtain the correct classical dynamics predicted by an electronic structure

100 Although classical electrostatics theory predicts that ions are r

101 hrough analysis of natural bond orbitals and classical electrostatics.

102 tor coeruleus made it a favorite subject for classical embryologists.

103 are secreted proteins, exported through the classical endoplasmic reticulum (ER)/Golgi-dependent pat

104 hase of angiogenesis was not associated with classical endothelial cell (EC) activation signs, such a

105 d in ammonium assimilation differed from the classical "enteric paradigm" for nitrogen utilization.

106 Using classical epidemiology and machine-learning methods in 1

107 l phosphorescence by highlighting studies of classical examples like molecular nitrogen and oxygen, b

108 The classical explanation for the gating compliance is that

109 negatively with the conditioning response in classical eyeblink conditioning in patients.

110 N215S does not lead to the development of a classical Fabry phenotype but induces a specific cardiac

111 PS cDKO mice display classical features of neurodegeneration occurring in Alz

112 ynaptic input, in hippocampal CA3 neurons, a classical focus for epileptogenesis.

113 ications that the FAM3C proteins do not form classical four-helix-bundle structures as was initially

114 induces the transition of the beta1AR from a classical Galphas-coupled receptor to a Galphai-coupled

115 nergic receptor (beta1AR) is recognized as a classical Galphas-coupled receptor.

116 ) equilibrium points whereby players in some classical games are always outperformed if sharing and p

117 t the highly surface-expressed M1 protein, a classical GAS virulence factor, was required for high-le

118 ingly, paternally-expressed genes of the non-classical gene imprinted network were strikingly enriche

119 Classical genetic studies identified five major SIX-ROWE

120 lioblastoma from poorly motile proneural and classical glioblastoma.

121 e residue flexibility when compared with the classical GNM and the parameter free GNM.

122 al results indicated that a variation of the classical GNMs by combining other protein structural pro

123 pal activity as disoriented mice performed a classical goal-directed spatial memory task in a rectang

124 B-type natriuretic peptide release; all are classical hallmarks of heart failure.

125 ndent of hypertension and is correlated with classical hemodynamic derangements that develop with str

126 ensin reveals that it occurs not only in the classical heteropentameric "monomer" form, but that it a

127 Patients had classical HL and were ineligible for or declined frontli

128 outcome, consistent with the known impact of classical HLA alleles.

129 nces of promoter region variation within the classical HLA class I loci.

130 nct from Hodgkin and Reed-Sternberg cells of classical Hodgkin lymphoma (CHL) (uniform CD50 and varia

131 Reed-Sternberg (RS) cells of classical Hodgkin lymphoma (cHL) express multiple immuno

132 ess of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti-PD-1 mon

133 of a variety of B-cell lymphomas, including classical Hodgkin lymphoma (cHL).

134 g (HRS) cells to evade antitumor immunity in classical Hodgkin lymphoma (cHL).

135 n patients with relapsed or refractory (R/R) classical Hodgkin lymphoma (HL).

136 ches and identifies new associations between classical human leukocyte antigen (HLA) alleles and comm

137 a radical mechanism, which is in contrast to classical Hunsdiecker-type decarboxylative halogenations

138 This work stands in contrast to classical hypotheses, which predict a positive effect of

139 sis and also to obviate biopsy in cases with classical imaging findings.

140 Beyond classical immune functions, they have been shown to be i

141 tically, this was not solely the result of a classical immune memory response, but rather involved lo

142 Mtb dormancy related (DosR) latency, but not classical immunodominant secretory antigens, to clearly

143 ) and CD8(+) T cells compared to a resistant classical inbred mouse strain.

144 me social unit is a critical missing term in classical inclusive fitness calculations (the "reproduct

145 e commonly described in mice and humans: the classical inflammatory monocytes, which are rapidly mobi

146 In distributed quantum and classical information processing, spatially separated pa

147 frontline immunomodulators categorized into classical, intermediate or non-classical subsets, and su

148 Monocytes are a diverse population of cells (classical, intermediate, and nonclassical) with distinct

149 loride intracellular channels (CLIC) are non-classical ion channels lacking a signal sequence for mem

150 ntable in any standard laboratory and with a classical ion trap mass spectrometer were other remarkab

151 as a previous pandemic strain of the biotype Classical is polymyxin-sensitive.

152 phy appears to be unhelpful, suggesting that classical iSS is not associated with macrovascular arter

153 Type 1 (classical) iSS, defined using simple radiological criter

154 efied gas flows is known to deviate from the classical laws of Navier and Fourier in Navier-Stokes-Fo

155 Classical learning algorithms, such as the delta rule wi

156 Classical learning theories predict extinction after the

157 Activation of the complement system via classical, lectin, or alternative pathways generates ana

158 rier for the highly exothermic reaction to a classical Lewis structure nevertheless make us optimisti

159 direct optical absorption measurement using classical light.

160 Classical lissencephaly is characterized by smooth cereb

161 1b1), also called Lissencephaly-1, can cause classical lissencephaly, a severe malformation of cortic

162 on shows inflated Type-I error rates but the Classical logistic and Bayes logistic (BL) regressions a

163 ed a transcriptional program distinct from a classical LPS response, pointing to unique P. falciparum

164 Like classical LTP, kainate-receptor-dependent LTP recruits r

165 rbor a 5' end modification distinct from the classical m(7)G cap that promotes rather than inhibits R

166 um interpolation can achieve spectroscopy of classical magnetic fields and individual quantum spins w

167 ii-Kosterlitz-Thouless phase transition, and classical magnetism, among the many systems that are des

168 It encodes the beta subunit of the non-classical major histocompatibility complex class II (MHC

169 chromatin requires C-terminal acetylation-a classical mark for transcriptionally active p53-and corr

170 Whereas the quality of classical MD force fields has improved significantly in

171 or purely nanomechanical resonators, even if classical mechanical analogies were referred from a theo

172 lectivity factor (E > 500), showing that the classical mechanism involving SN2 reaction by Asp110 per

173 gardless of tumor development subtype (i.e., classical, mesenchymal, neural, proneural).

174 This Review focuses on classical metal ion modeling based on unpolarized models

175 Halofunctionalization of alkenes is a classical method for olefin difunctionalization.

176 s that merge all of the tedious steps of the classical methods into a simple, efficient, and low-cost

177 mpetitive alternative to metal catalyzed and classical methods of preparing benzoxazinone.

178 saturating conditions are not limited to the classical methylotrophic pathway.

179 neutralizing antibodies independently of the classical MHC haplotype.

180 The enzyme exhibits classical Michaelis-Menten kinetics and acts cooperative

181 The classical model assumes precipitation in contrast with o

182 Some of these models include the classical model based on Jacobson-Stockmayer polymer the

183 A semi-classical model of the spin-polarization dynamics of bal

184 produces the experimental results, whereas a classical model only predicts a red shift.

185 particular focus on how these methods inform classical modeling efforts.

186 ns are offered that will further enhance the classical modeling of metal ion-containing systems.

187 electronic detection method in comparison to classical molecular biological assays.

188 These methodologies range from classical molecular biology and optical approaches, such

189 We use classical molecular dynamics and hybrid quantum mechanic

190 Structures calculated using classical molecular dynamics are in excellent agreement

191 bining the phase field crystal approach with classical molecular dynamics simulations and quantum-mec

192 onance energy transfer (smFRET) experiments, classical molecular dynamics simulations, and nucleotide

193 ction, we employ here multiscale quantum and classical molecular simulations.

194 alysis of speeds of sound in ILs vs those in classical molecular solvents is presented to compare the

195 of blood monocyte subsets indicates that non-classical monocytes are biased progenitors of alternativ

196 vivo deuterium labeling, we demonstrate that classical monocytes emerge first from marrow, after a po

197 nocytes was achieved by the early release of classical monocytes from bone marrow.

198 acerbated M2-skewed immunosuppression of non-classical monocytes in conjunction with a global suppres

199 ng growth factor beta alone, whereas CD14(+) classical monocytes required additional notch ligation.

200 In contrast, classical monocytes secreted high levels of IL-6, the bl

201 olecule FTY720 recruits S1PR3-expressing non-classical monocytes that support vascular remodeling aft

202 Both heterogeneity of classical MPNs and prognosis are determined by a specifi

203 hat of CAACs and similar to that observed in classical N-heterocyclic carbenes.

204 no correlation between repeat occurrence and classical network states such as theta oscillations and

205 sion of the ALDH gene ALDH1A2 Interestingly, classical NFkappaB signaling through the RelA transcript

206 AChR) in a cooperative fashion, not seen for classical nicotinic agonists and antagonists.

207 Although a classical NLS and importin alpha/beta mediated nuclear i

208 e recovery of the binary star underlying the classical nova eruption of 11 March AD 1437, and indepen

209 up to one million times that of the Sun, all classical novae are recurrent, on timescales of months t

210 The three other oldest recovered classical novae display nova shells, but lack firm post-

211 ries-classical capillarity for intrusion and classical nucleation theory (CNT) for extrusion-because

212 As a consequence, heterogeneous classical nucleation theory cannot describe our simulati

213 We use classical nucleation theory to show that the freezing ef

214 orders of magnitude higher than predicted by classical nucleation theory.

215 tion of ZnO NPs on CT activity, here we used classical (O395) and El Tor (C6706) V. cholerae biotypes

216 We successfully validated it as a model for classical OI.

217 fibers (FMFs) have been recently employed in classical optical communication to increase the data tra

218 A single-photon or classical optical pulse as the gate sets the spin state

219 with PSC studied, 65.5% were men, 89.8% had classical or large-duct disease, and 70.0% developed IBD

220 ex (low flow) and low-gradient with reduced (classical) or preserved (paradoxical) ejection fraction.

221 let surface, which cannot be synthesized via classical organic chemistry the triplet non-aromatic 2,4

222 Classical osteogenesis imperfecta (OI) is a bone disease

223 ect reduction of the oxorhenium(VII) moiety (classical oxygen atom transfer) rather than through init

224 A promising therapeutic approach may be classical pathway (CP) inhibition at the level of early

225 l hemolysis after forceful activation of the classical pathway could be reduced by blocking the AP.

226 Together, these data suggest that the classical pathway plays a major role in complement activ

227 ent C1q and activation of complement via the classical pathway without any concomitant engagement of

228 own to interact with other activators of the classical pathway.

229 s predictive as FAI for the diagnosis of the classical PCOS phenotype, and the combination of salT or

230 Here, we used classical pharmacology, in situ hybridization, immunohis

231 ow-absorbance transition formerly ignored in classical photochemistry has been found for maleimides.

232 y a factor of 7.47 under preservation of non-classical photon-number statistics.

233 nopsin with synaptically mediated drive from classical photoreceptors through bipolar-cell input.

234 ctively reversed associative LTF, while a dn classical PKM selectively reversed non-associative LTF.

235 iffusion coefficients are consistent and the classical PNP equations with renormalized coefficients a

236 Classical postulated mechanisms for bronchial obstructio

237 uring range expansions (which acknowledges a classical prediction).

238 The clinical phenotype ranges from the classical presentation of a congenital myasthenic syndro

239 The effect of these SNPs is independent of classical prognostic factors and there is no heterogenei

240 nd presenting heterogeneous phenotypes, from classical proinflammatory M1 to alternative anti-inflamm

241 incided with DNA hypomethylation and gain of classical promoter histone marks, while HDACi specifical

242 haracteristics of the proteasome and HslV, a classical proteasomal reaction mechanism could be inferr

243 Classical protein-tyrosine phosphatases can exhibit subs

244 ormance on a novel gaze perception task with classical psychophysical metrics (precision and accuracy

245 ilizing the binding features of CyP6Q[6] and classical Q[7].

246 erimental results and demonstrate a combined classical/quantum approach to perform realistic modeling

247 D177 expression pattern that does not follow classical random monoallelic expression or imprinting.

248 suppressed by stimuli that extend beyond the classical receptive field.

249 ed intracellular domain (ICD) in addition to classical receptor tyrosine kinase-activated signaling c

250 This introduces computational challenges for classical relational databases, due to the sparsity and

251 SAWs being described by a relatively simple classical relaxation model.

252 umoebavirus, that is most closely related to classical representatives of the Asfarviridae family.

253 aminidase's functionality extends beyond its classical role in influenza virus infection and that ant

254 re, we show that AChE plays an essential non-classical role in vertebrate gut morphogenesis.

255 y with the three cryptic inscriptions of the classical Rosetta Stone, the Hechtian Hypothesis transla

256 eral phylogenomic studies have supported the classical scenario in which sponges (Porifera) are the s

257 vestigated effects of OA on the skeleton of "classical" sea urchins (euechinoids), but the impact of

258 ntum computer with a well-known speedup over classical searches of an unsorted database.

259 esource theories of quantum entanglement and classical secret key.

260 Non-classical secretory vesicles, collectively referred to a

261 amma rays seen in EM170817 are dissimilar to classical short gamma-ray bursts with ultrarelativistic

262 is the dominant calcium sensor required for classical short-term neutrophil responses.

263 cal reactions; (2) illustrate the ability of classical simulations to correctly interpret and predict

264 0.781 Ma is possible, the precise age of the classical site at SZ is still controversial.

265 r protein recognition that are orthogonal to classical small molecule and protein-based approaches.

266 MIPs have been intensively employed in classical solid-phase extraction and solid-phase microex

267 and Dy2Ti2O7, so-called spin ices, exhibit a classical spin liquid state with fractionalized thermal

268 The sensor array was developed from classical spot tests using aniline and phenylhydrazine d

269 The deterministic generation of non-classical states of light, including squeezed states, Fo

270 c resources contained in general quantum and classical states.

271 egorized into classical, intermediate or non-classical subsets, and subsequently differentiated into

272 subset of tumors within the "proneural" and "classical" subtypes that are addicted to aberrant signal

273 dividuals with FN1 mutations from those with classical Sutcliffe-type SMD.

274 Classical swine fever (CSF) is a notifiable, highly cont

275 Surveillance of Classical Swine Fever (CSF) should not only focus on liv

276 e the IIId2 sub-domains of two pestiviruses, classical swine fever virus (CSFV) and border disease vi

277 which have been impossible to access through classical synthetic methods.

278 m has turned into a diffusive collision-full classical system.

279 qualitatively different from the equivalent classical system?

280 However, in classical systems, no direct experimental observation of

281 hat have explored integrated signaling among classical TH 2 cytokines (IL-4, IL-5, and IL-13), which

282 Although the demonstration is classical, the same technique can be used to generate en

283 hanges, do not match the expectations of the classical theories.

284 rimental evidence of kink blocking validates classical theory and demonstrates that this mechanism is

285 a planar vertex model that exhibits no bulk classical thermodynamic phase transition, independent of

286 reated as part of an undergraduate course of classical thermodynamics or modern physics, the review a

287 Stochastic thermodynamics extends classical thermodynamics to small systems in contact wit

288 are predicted to deviate substantially from classical thermodynamics.

289 -14 Hz), even when this rate went beyond the classical theta range (4-8 Hz).

290 cfDNA-triggered NETosis is independent of classical TLR9 signaling.

291 ompared their responses to known features of classical Tmem.

292 Unlike the classical twinning route, deformation twinning initiated

293 The products display classical UV-vis electronic spectra of carbo-benzenes in

294 y more sensitive to temperature change, than classical vesicles.

295 The classical view of hydrophobic hydration is that, in the

296 The classical view of therapeutic monoclonal antibodies (mAb

297 le, structure, and genomes break the mold of classical viruses.

298 ) to considerably improve the performance of classical wastewater treatment technologies, e.g. adsorp

299 Classical ways of manipulating PI(4,5)P2 levels are slow

300 gment sized primary benzenesulfonamides, the classical zinc binding group found in most CA II inhibit